{
    "disease_id": "DOID:0110841", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "Usher syndrome caused by mutation in CLRN1"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "USH3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "USHER syndrome, type IIIA; USH3A"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "CLRN1 Usher syndrome"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "Usher syndrome type IIIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "Usher syndrome, type 3"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "USHER syndrome, type IIIA"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0010170", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0010170", 
            "name": "Usher syndrome, type 3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110841", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110841", 
            "name": "USH3A"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:0110841", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:0110841", 
            "name": "Usher syndrome type IIIA"
        }, 
        {
            "url": "https://www.omim.org/entry/276902", 
            "description": "", 
            "resource": "MIM", 
            "id": "MIM:276902", 
            "name": "Usher syndrome 3A"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:0110841", 
        "description": "An Usher syndrome type 3 that has_material_basis_in homozygous or compound heterozygous mutation in the CLRN1 gene on chromosome 3q25.", 
        "resource": "Disease Ontology", 
        "id": "DOID:0110841", 
        "name": "Usher syndrome type 3A"
    }, 
    "evidence": [
        {
            "url": "https://www.omim.org/entry/276902", 
            "id": "276902", 
            "database": "MIM"
        }
    ]
}